Search results for "Time-resolved spectroscopy"

showing 10 items of 39 documents

Polyamine Linear Chains Bearing Two Identical Terminal Aromatic Units. Evidence for a Photo Induced Bending Movement

2001

Abstract Several chemosensors bearing a fluorescent unit at both ends of a linear polyamine chain were synthesised. The protonation as well as the association constants with Cu2+ and Zn2+ were determined by potentiometry in 0.15 mol dm−3 NaCl at 298.1 K. In the case of 1,16-bis(1-naphthylmethyl)-1,4,7,10,13,16-hexaazadecane hexahydrochloride (L1), formation of an excimer emission in aqueous acidic solutions was observed. The system was characterized by steady state fluorescence emission and by time resolved fluorescence. In the ground state the molecule is expected to adopt a more or less linear conformation, while in the excited state a bending movement of the chain must occur in order to …

Aqueous solutionChemistryExcited stateMoleculeProtonationGeneral ChemistryTime-resolved spectroscopyExcimerPhotochemistryGround stateFluorescenceSupramolecular Chemistry
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<title>Time-resolved fluorescence study of interaction of the monoclonal anticoproporphyrin antibodies and (Pt-)coproporphyrin</title>

1995

Mechanisms of ligand binding by monoclonal anti-coproporphyrin antibodies are studied by steady-state and time-resolved fluorescence spectroscopy by use of a picosecond laser system. The antibodies quench the coproporphyrin (CP) fluorescence, but the CP fluorescence spectra show a strong shift of maxima at high concentrations of antibodies (Ab) or their Fab fragment. This can be explained by a special type of Ab or Fab dimerization. Fluorescence decays of CP are measured at different concentrations of Ab and different pH values. The following deconvolution procedure based on the non-linear least squares method reveals a two- exponential character of the fluorescence decay. Data obtained by …

ChemistryAnalytical chemistryFluorescence cross-correlation spectroscopyTime-resolved spectroscopySpectroscopyLaser-induced fluorescenceLuminescencePhosphorescenceFluorescenceFluorescence spectroscopySPIE Proceedings
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Up-conversion processes in NaLaF4:Er3+

2009

abstract Structural and spectroscopic investigation of NaLaF 4 :Er 3+ material at different doping concentrations ispresented. X-ray diffraction patterns, up-conversion luminescence spectra and decay curves for 2 H 9/2 ? 4 I 15/2 , 4 S 3/2 ? 4 I 15/2 and 4 F 9/2 ? 4 I 15/2 optical transitions in the material are shown and possibleexcitation routes are discussed. Raman spectrum for the undoped material is presented and the effectivephonon energy of the material is estimated. Based on the obtained results application of rare-earth dopedNaLaF 4 in the field of up-conversion phosphors is evaluated. 2009 Elsevier B.V. All rights reserved. 1. IntroductionFor many years rare-earth (RE) doped materi…

ChemistryOrganic ChemistryDopingAnalytical chemistryNonlinear opticsPhosphorAtomic and Molecular Physics and OpticsPhoton upconversionElectronic Optical and Magnetic MaterialsIonInorganic Chemistrysymbols.namesakesymbolsElectrical and Electronic EngineeringPhysical and Theoretical ChemistryAtomic physicsTime-resolved spectroscopyLuminescenceRaman spectroscopySpectroscopyOptical Materials
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Characterisation of Chlorophyll a and Chlorophyll b Monomers in Various Solvent Environments with Ultrafast Spectroscopy

1998

In photosynthesis the energy from the sun is captured by light harvesting chlorophyll pigments and converted to stable chemical energy, by the photochemical reaction center. Photosynthetic energy transfer in the antenna systems of green plants has previously been studied by ultrafast time resolved spectroscopy. The characteristics of the chlorophyll pigments itself is important to study in order to understand the dynamics on a femtosecond timescale. One way to study the energy transfer is to use transient absorption spectroscopy and follow the increase or decrease in the transient absorption signal with time (1). Another way to study the energy transfer is to monitor the change in dichroism…

Chlorophyll bPhysics::Biological Physics0303 health sciencesChlorophyll aMaterials scienceDichroism010402 general chemistryPhotochemistry7. Clean energy01 natural sciences0104 chemical sciencesLight-harvesting complex03 medical and health scienceschemistry.chemical_compoundchemistryChlorophyllUltrafast laser spectroscopyTime-resolved spectroscopySpectroscopy030304 developmental biology
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Ultrafast Metamorphosis of a Complex Charge Density Wave in Tantalumdiselenite

2016

Using ultrafast electron diffraction, we record the transformation between a nearly-commensurate and an incommensurate charge-density-wave in 1T-TaS2, which takes place orders of magnitude faster than previously observed for commensurate-to-incommensurate transitions.

Condensed Matter::Quantum GasesDiffractionPhysicsOrders of magnitude (temperature)Ultrafast electron diffractionmedia_common.quotation_subjectPhysics::OpticsCondensed Matter::SuperconductivityElectric fieldCondensed Matter::Strongly Correlated ElectronsAtomic physicsTime-resolved spectroscopyMetamorphosisCharge density waveUltrashort pulsemedia_commonInternational Conference on Ultrafast Phenomena
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Application of time-resolved spectroscopy to concentration measurements in gas mixtures

2001

1296-2147; Concentration measurements using femtosecond Raman Induced Polarization Spectroscopy (RIPS) are performed in binary gas mixtures CO2-N2 and CO2-N2O at room temperature. The principle of these measurements is based on the nonlinear rotational time response of each molecular component of the mixture, The general form of this molecular response is a series of periodic transients with a period related to the rotational constant Be The relative strength of the individual responses allows an accurate determination of the concentration. Two techniques are presented using either two pulses (one pump and one probe) or three pulses (two pumps and one probe). (C) 2001 Academie des sciences/…

DYNAMICSmolecular concentrationMaterials scienceAnalytical chemistryGeneral Physics and Astronomy01 natural sciencesInduced polarizationsymbols.namesakeINDUCED POLARIZATION SPECTROSCOPYfemtosecond laser0103 physical sciencesMOLECULE010306 general physicsSpectroscopyPOPULATIONINTERFERENCE010304 chemical physicsTriatomic moleculeFEMTOSECONDDiatomic moleculeINVERSE RAMAN-SPECTROSCOPYROTATIONAL COHERENCEFemtosecondsymbolsCO2Rotational spectroscopyTime-resolved spectroscopyRaman spectroscopystimulated Raman effect
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Concentration measurements in molecular gas mixtures with a two-pump pulse femtosecond polarization spectroscopy technique

2001

0021-9606; Recently, we have demonstrated the ability of the Raman-induced polarization spectroscopy (RIPS) technique to accurately determine concentration or polarizability anisotropy ratio in low-pressure binary molecular mixtures [E. Hertz, B. Lavorel, O. Faucher, and R. Chaux, J. Chem. Phys. 113, 6629 (2000)]. It has been also pointed out that macroscopic interference, occurring when two revivals associated to different molecules time overlap, can be used to achieve measurements with picosecond time resolution. The applicability of the technique is intrinsically limited to a concentration range where the signals of both molecules are of the same magnitude. In this paper, a two-pump puls…

INTERFERENCEDYNAMICS010304 chemical physicsChemistrybusiness.industryGeneral Physics and AstronomyPulse sequenceTRANSITIONSPolarization (waves)01 natural sciencesMolecular physicsROTATIONAL COHERENCEOpticsPolarizabilityPicosecond0103 physical sciencesFemtosecondCO2Physical and Theoretical ChemistryTime-resolved spectroscopy010306 general physicsSpectroscopyAnisotropybusinessPOPULATION
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Photoluminescence study of terbium-exchanged ultrastable Y zeolites: Number of species, photoluminescence decays and decay-associated spectra

2008

Terbium-exchanged ultrastable Y (USY) zeolites were investigated by using time-resolved photoluminescence spectroscopy techniques and methods. To determine the distribution of terbium species in USY zeolites together with their photoluminescence properties, several analysis methods for the time-resolved luminescence spectra were used such as the area normalization of time-resolved photoluminescence spectra, singular value decomposition, global nonlinear least squares, and the maximum entropy. Except for a questionable long lifetime, small contribution of a terbium species with lifetime of 1.9¿2.1 ms, all the experimental and analysis results converged to a two terbium species distribution w…

LanthanidePhotoluminescenceSilylationAnalytical chemistryFísicaGeneral Physics and Astronomychemistry.chemical_elementTerbiumQuímica analíticaCiència dels materialsSpectral linechemistryNon-linear least squaresInstitut für ChemieTime-resolved spectroscopySpectroscopy
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Mixed complexes of alkaline earth uranyl cabonates: A laser-induced time-resolved fluorescence spectroscopic study

2008

The interaction of the alkaline earth ions Mg2+, Sr2+ and Ba2+ with the uranyl tricarbonate complex has been studied by time resolved laser-induced fluorescence spectroscopy. In contrast to the non-luminescent uranyl tricarbonate complex the formed products show slight luminescence properties. These have been used to determine the stoichiometry and complex stabilities of the formed compounds. As the alkaline earth elements are located in an outer shell of the complex the influence of the type of the alkaline earth element on the stability constant is not very drastic. Therefore all obtained data were averaged in order to derive an common stability constant for the described complexes. These…

LuminescenceLightAnalytical chemistryCarbonateschemistry.chemical_elementFluorescence spectroscopyAnalytical ChemistryPhosphatesuraniumchemistry.chemical_compoundAlkaline earth elementscarbonatecomplex formationluminescenceMagnesiumInstrumentationSpectroscopyIonsAlkaline earth metalModels StatisticalTemperatureBariumHydrogen-Ion ConcentrationUranylAtomic and Molecular Physics and OpticsCarbonSpectrometry FluorescencechemistryStability constants of complexesBariumStrontiumUraniumTime-resolved spectroscopyLuminescenceStoichiometry
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Wide range excitation of visible luminescence in nanosilica

2010

The visible luminescence of nanometer-sized silica particles (7 nm mean diameter) was investigated using time resolved spectroscopy. This luminescence is characterized by a wide excitation in the visible and ultraviolet range. The emission spectrum is centred at 2.72 eV with a full width at half maximum of 0.70 eV when excited above 3.5 eV, whereas it progressively empties on the high energy side when excited below 3.5 eV. Moreover, the lifetime falls in the ns timescale and decreases on increasing the emission energy. These features are due to the exceptionally broad inhomogeneous distribution of the emitting centres peculiar to the silica nanoparticles. © 2010 Elsevier B.V. All rights res…

Materials Chemistry2506 Metals and AlloysRange (particle radiation)PhotoluminescenceMaterials scienceoptical down conversionChemistry (all)General ChemistrynanosilicaCondensed Matter PhysicCondensed Matter PhysicsA. NanostructureD. Optical propertieFull width at half maximumC. Point defectExcited stateMaterials ChemistryluminescenceSpontaneous emissionEmission spectrumAtomic physicsTime-resolved spectroscopyE. LuminescenceLuminescence
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